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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503801Generated: October 30, 2026

Triethylborane → 3-Chloro-5-ethylbenzaldehyde

https://huagongshe.com/reaction/1503801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylboraneHCID 7357—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Bromo-5-chlorobenzaldehydeHCID 17750952—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-Chloro-5-ethylbenzaldehydeHCID 8408307842.9%

Reaction Steps

PdCl2(dppf) (37 mg, 0.046 mmol), potassium phosphate (1.93 g, 9.11 mmol) and triethylborane (1M in hexane, 0.45 g, 4.56 mmol) were added to a solution of 3-bromo-5-chloro-benzaldehyde (1.0 g, 4.56 mmol) in THF (20 mL) at ambient temperature and the mixture was refluxed for 12 h. The reaction mixture was brought to ambient temperature, diluted with EtOAc and washed with water. The organic layer was dried (Na2SO4), filtered, concentrated and the residue was purified by column chromatography on silica (100-200 mesh) eluting with 2% EtOAc in petroleum ether to afford the title compound (330 mg, 41%) as a pale yellow liquid: 1H NMR (400 MHz, DMSO-d6) δ 9.97 (s, 1H), 7.75 (d, J=1.6 Hz 1H), 7.73 (s, 1H), 7.65 (s, 1H), 2.74-2.68 (m, 2H), 1.23 (t, J=7.6 Hz, 3H); ESIMS m/z 168.0 ([M]+); IR (thin film) 3071, 1699, 692 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212164B2
Source datasetuspto-grants-2015_12
ORD IDord-db80a8333a1c4a57a4fae3b0bb34a8bb
Source noteuspto-grants-2015_12